In the standard self-consistent field theory (SCFT), a polymer chain is modeled as an infinitely flexible Gaussian chain, and the partition function is calculated by solving a differential equation in the form of a modified diffusion equation. The Gaussian chain assumption makes the standard SCFT inappropriate for modeling of short polymers, and the discrete chain SCFT in which the partition function is obtained through recursive integrals has recently been suggested as an alternative method. However, the shape of the partition function integral makes this method much slower than the standard SCFT when calculated in the real space.
View Article and Find Full Text PDFACS Appl Mater Interfaces
June 2019
A nanosquare array is an indispensable element for the integrated circuit design of electronic devices. Block copolymer (BCP) lithography, a promising bottom-up approach for sub-10 nm patterning, has revealed a generic difficulty in the production of square symmetry because of the thermodynamically favored hexagonal packing of self-assembled sphere or cylinder arrays in thin-film geometry. Here, we demonstrate a simple route to square arrays via the orthogonal self-assembly of two lamellar layers on topographically patterned substrates.
View Article and Find Full Text PDFFor the purpose of checking material conservation of various numerical algorithms used in the self-consistent-field theory (SCFT) of polymeric systems, we develop an algebraic method using matrix and bra-ket notation, which traces the Hermiticity of the product of the volume and evolution matrices. Algebraic tests for material conservation reveal that the popular pseudospectral method in the Cartesian grid conserves material perfectly, while the finite-volume method (FVM) is the proper tool when real-space SCFT with the Crank-Nicolson method is adopted in orthogonal coordinate systems. We also find that alternating direction implicit methods combined with the FVM exhibit small mass errors in the SCFT calculation.
View Article and Find Full Text PDFWe systematically examined the polymer-mediated interparticle interactions between polymer-grafted nanoparticles (NPs) within chemically identical homopolymer matrices through experimental and computational efforts. In experiments, we prepared thermally stable gold NPs grafted with polystyrene (PS) or poly(methyl methacrylate) (PMMA), and they were mixed with corresponding homopolymers. The nanocomposites are well dispersed when the molecular weight ratio of free to grafted polymers, α, is small.
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